ZFIN ID: ZDB-PERS-130130-1
Schimmenti, Lisa A.
Email: las@umn.edu
URL: http://www.med.umn.edu/peds/genetics/faculty/schimmentilisa/home.html
Affiliation: Schimmenti Lab
Address: University of Minnesota Department of Pediatrics 420 Delaware Street SE MMC 730 Minneapolis, Minnesota 55455
Country: United States
Phone: 612-624-5613
Fax: 612-626-2993
ORCID ID:


BIOGRAPHY AND RESEARCH INTERESTS


PUBLICATIONS
Koleilat, A., Dugdale, J.A., Christenson, T.A., Bellah, J.L., Lambert, A.M., Masino, M.A., Ekker, S.C., Schimmenti, L.A. (2020) L-type voltage-gated calcium channel agonists mitigate hearing loss and modify ribbon synapse morphology in the zebrafish model of Usher syndrome type 1. Disease models & mechanisms. 13(11):
Muthusamy, K., Hanna, C., Johnson, D.R., Cramer, C.H., Tebben, P.J., Libi, S.E., Poling, G.L., Lanpher, B.C., Morava, E., Schimmenti, L.A. (2020) Growth hormone deficiency in a child with branchio-oto-renal spectrum disorder: Clinical evidence of EYA1 in pituitary development and a recommendation for pituitary function surveillance. American journal of medical genetics. Part A. 185(1):261-266
Ichino, N., Serres, M.R., Urban, R.M., Urban, M.D., Treichel, A.J., Schaefbauer, K.J., Greif, L.E., Varshney, G.K., Skuster, K.J., McNulty, M.S., Daby, C.L., Wang, Y., Liao, H.K., El-Rass, S., Ding, Y., Liu, W., Anderson, J.L., Wishman, M.D., Sabharwal, A., Schimmenti, L.A., Sivasubbu, S., Balciunas, D., Hammerschmidt, M., Farber, S.A., Wen, X.Y., Xu, X., McGrail, M., Essner, J.J., Burgess, S.M., Clark, K.J., Ekker, S.C. (2020) Building the vertebrate codex using the gene breaking protein trap library. eLIFE. 9:
Riché, R., Liao, M., Pena, I.A., Leung, K.Y., Lepage, N., Greene, N., Sarafoglou, K., Schimmenti, L.A., Drapeau, P., Samarut, É. (2018) Glycine decarboxylase deficiency-induced motor dysfunction in zebrafish is rescued by counterbalancing glycine synaptic level. JCI insight. 3(21):
Schimmenti, L.A. (2017) Tank to Bedside: Zebrafish and the Cancer Moonshot. Zebrafish. 14(4):390-392
Schimmenti, L. (2017) Correction to: Zebrafish 2016;13:545-547. Zebrafish. 14:195
Shaw, N.D., Brand, H., Kupchinsky, Z.A., Bengani, H., Plummer, L., Jones, T.I., Erdin, S., Williamson, K.A., Rainger, J., Stortchevoi, A., Samocha, K., Currall, B.B., Dunican, D.S., Collins, R.L., Willer, J.R., Lek, A., Lek, M., Nassan, M., Pereira, S., Kammin, T., Lucente, D., Silva, A., Seabra, C.M., Chiang, C., An, Y., Ansari, M., Rainger, J.K., Joss, S., Smith, J.C., Lippincott, M.F., Singh, S.S., Patel, N., Jing, J.W., Law, J.R., Ferraro, N., Verloes, A., Rauch, A., Steindl, K., Zweier, M., Scheer, I., Sato, D., Okamoto, N., Jacobsen, C., Tryggestad, J., Chernausek, S., Schimmenti, L.A., Brasseur, B., Cesaretti, C., García-Ortiz, J.E., Buitrago, T.P., Silva, O.P., Hoffman, J.D., Mühlbauer, W., Ruprecht, K.W., Loeys, B.L., Shino, M., Kaindl, A.M., Cho, C.H., Morton, C.C., Meehan, R.R., van Heyningen, V., Liao, E.C., Balasubramanian, R., Hall, J.E., Seminara, S.B., Macarthur, D., Moore, S.A., Yoshiura, K.I., Gusella, J.F., Marsh, J.A., Graham, J.M., Lin, A.E., Katsanis, N., Jones, P.L., Crowley, W.F., Davis, E.E., FitzPatrick, D.R., Talkowski, M.E. (2017) SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome. Nature Genetics. 49(2):238-248
Schimmenti, L.A. (2016) Keep Swimming Toward Precision Medicine Discoveries. Zebrafish. 13:545-547
Pei, W., Xu, L., Varshney, G.K., Carrington, B., Bishop, K., Jones, M., Huang, S.C., Idol, J., Pretorius, P.R., Beirl, A., Schimmenti, L.A., Kindt, K.S., Sood, R., Burgess, S.M. (2016) Additive reductions in zebrafish PRPS1 activity result in a spectrum of deficiencies modeling several human PRPS1-associated diseases. Scientific Reports. 6:29946
Schimmenti, L.A. (2016) Zebrafish: A Functional Refuge at the End of an Odyssey. Zebrafish. 13(3):236-8
Tye, M., Rider, D., Duffy, E.A., Seubert, A., Lothert, B., Schimmenti, L.A. (2015) Nonhatching Decapsulated Artemia Cysts As a Replacement to Artemia Nauplii in Juvenile and Adult Zebrafish Culture. Zebrafish. 12(6):457-61
Duffy, E.A., Pretorius, P.R., Lerach, S., Lohr, J.L., Hirsch, B., Souza, C.M., Veillette, A., Schimmenti, L.A. (2015) Mosaic partial deletion of PTPN12 in a child with interrupted aortic arch type A. American journal of medical genetics. Part A. 167(11):2674-83

NON-ZEBRAFISH PUBLICATIONS